Ranitidine
Ranitidine Tablets, USP
Approved
Approval ID
b85c7258-f5a2-4baa-b2e5-f951da7589e9
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 13, 2010
Manufacturers
FDA
State of Florida DOH Central Pharmacy
DUNS: 829348114
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ranitidine
PRODUCT DETAILS
NDC Product Code53808-0775
Application NumberANDA077824
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateApril 13, 2010
Generic NameRanitidine
INGREDIENTS (1)
RANITIDINE HYDROCHLORIDEActive
Quantity: 150 mg in 1 1
Code: BK76465IHM
Classification: ACTIB